首页> 外文期刊>International journal of colorectal disease. >TCF-3, 4 protein expression correlates with beta-catenin expression in MSS and MSI-H colorectal cancer from HNPCC patients but not in sporadic colorectal cancers.
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TCF-3, 4 protein expression correlates with beta-catenin expression in MSS and MSI-H colorectal cancer from HNPCC patients but not in sporadic colorectal cancers.

机译:在来自HNPCC患者的MSS和MSI-H大肠癌中,TCF-3、4蛋白表达与β-catenin表达相关,而在散发性大肠癌中则不相关。

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PURPOSE: The beta-catenin-T-cell factor-4 (TCF-4) complex is the main control switch of cell proliferation and differentiation of normal and malignant intestinal cells. The aim of our study was to analyze the protein expression of components of the Wnt pathway in microsatellite stable (MSS) and highly unstable (MSI-H) sporadic and hereditary nonpolyposis colorectal cancer (HNPCC) in human colorectal cancers. METHODS: Sixty seven colorectal tumors comprising of 15 sporadic MSS, 12 sporadic microsatellite instability colorectal tumors and 40 tumors from HNPCC patients, of which 20 were MSS and 20 MSI-H, were analyzed for the expression of APC, beta-catenin, and TCF-3, 4 proteins by immunohistochemistry. RESULTS: We found a significant difference in cytoplasmic APC expression frequency between sporadic MSS (52%) and HNPCC tumors (78%), whereas no difference was detected between MSI-H and MSS or HNPCC tumors. All tumor groups showed a similar pattern of decreased membranous staining and increased cytoplasmic and nuclear staining for beta-catenin compared to normal cells. Moreover, the TCF-3, 4 protein expression was higher (43%) in HNPCC-associated MSS tumors compared to sporadic tumors (14%; analysis of variance (ANOVA) p < 0.05). For HNPCC tumors, the subcellular beta-catenin expression (membranous, cytoplasmic, and nuclear) correlated with the nuclear TCF-3, 4 signal in MSS tumors (Spearman correlation p < 0.0007) and MSI-H tumors (Spearman correlation p < 0.0001). CONCLUSION: We have shown a previously unknown difference in TCF-3, 4 protein expression between sporadic and HNPCC MSS tumors. In addition, we found no difference in nuclear beta-catenin signal intensity, which may be caused by an alteration in Wnt pathway in MSS sporadic tumors by unknown mechanisms leading to lower TCF-3, 4 protein expression. This hypothesis has to be tested in future investigations.
机译:目的:β-catenin-T细胞因子4(TCF-4)复合物是正常和恶性肠道细胞增殖和分化的主要控制开关。我们研究的目的是分析人结肠直肠癌中的微卫星稳定(MSS)和高度不稳定(MSI-H)散发性和遗传性非息肉性结直肠癌(HNPCC)中Wnt通路成分的蛋白表达。方法:分析了包括15例散发性MSS,12例散发性微卫星不稳定性结直肠癌和40例HNPCC患者的67例大肠肿瘤中APC,β-catenin和TCF的表达,其中20例为MSS和20例MSI-H。 -3,通过免疫组化的4蛋白。结果:我们发现散发性MSS(52%)和HNPCC肿瘤(78%)之间的细胞质APC表达频率有显着差异,而MSI-H和MSS或HNPCC肿瘤之间没有发现差异。与正常细胞相比,所有肿瘤组均表现出相似的减少β-catenin膜膜染色,增加细胞质和核染色的模式。此外,与散发性肿瘤相比,HNPCC相关MSS肿瘤中TCF-3、4蛋白的表达更高(43%)(14%;方差分析(ANOVA)p <0.05)。对于HNPCC肿瘤,MSS肿瘤(Spearman相关性p <0.0007)和MSI-H肿瘤(Spearman相关性p <0.0001)中亚细胞β-catenin的表达(膜,胞质和核)与核TCF-3,4信号相关。 。结论:我们已经显示了散发性和HNPCC MSS肿瘤之间TCF-3、4蛋白表达的以前未知的差异。此外,我们发现核β-catenin信号强度没有差异,这可能是由于未知机制导致MSS散发性肿瘤中Wnt途径的改变导致TCF-3、4蛋白表达降低所致。该假设必须在以后的研究中进行检验。

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